TABLE 1.

ChIP-seq data alignment information

ChIP	No. of reads			% aligned	% uniquea	% genome coverage
	Total	Aligned	Unique
Input	54,990,464	35,623,672	32,940,684	64.78	92.47	90.64
H3	71,828,757	37,798,741	30,151,960	52.62	79.77	82.96
H3K9me3	84,339,867	39,799,707	27,591,619	47.19	69.33	75.92
H3K9ac	67,856,707	48,595,679	34,042,406	71.62	70.05	93.67
H4K5ac	66,596,815	46,239,262	34,065,138	69.43	73.67	93.73
H4K8ac	79,795,471	48,838,021	29,541,448	61.20	60.49	81.28
H4K12ac	71,252,246	46,341,541	33,485,169	65.04	72.26	92.14
H4K16ac	77,287,145	49,326,598	28,973,938	63.82	58.74	79.72
H4ac	70,049,830	48,662,721	32,799,658	69.47	67.40	90.25
BRD4	84,730,635	47,671,985	24,864,246	56.26	52.16	68.41

^aTotal aligned reads compared to uniquely mapped reads for each ChIP-seq sample.